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Cited by in F6Publishing

For:	Yan L, Shen R, Cao Z, Han C, Zhang Y, Liu Y, Yang X, Xie M, Li H. A Novel Missense Variant in the Gene PPP2R5D Causes a Rare Neurodevelopmental Disorder with Increased Phenotype. Biomed Res Int 2021;2021:6661860. [PMID: 33628804 DOI: 10.1155/2021/6661860] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]

For:

Yan L, Shen R, Cao Z, Han C, Zhang Y, Liu Y, Yang X, Xie M, Li H. A Novel Missense Variant in the Gene PPP2R5D Causes a Rare Neurodevelopmental Disorder with Increased Phenotype. Biomed Res Int 2021;2021:6661860. [PMID: 33628804 DOI: 10.1155/2021/6661860] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]

Number	Citing Articles
1	Liu R, Huang Y, Li C, Wang P, Wang Y, Zhang L. A novel nonsense mutation in PPP2R5D is associated with neurodevelopmental disorders and shows incomplete penetrance in a Chinese pedigree. Clinical Neurology and Neurosurgery 2022. [DOI: 10.1016/j.clineuro.2022.107524] [Reference Citation Analysis]
2	Vaneynde P, Verbinnen I, Janssens V. The role of serine/threonine phosphatases in human development: Evidence from congenital disorders. Front Cell Dev Biol 2022;10:1030119. [DOI: 10.3389/fcell.2022.1030119] [Reference Citation Analysis]
3	Verbinnen I, Vaneynde P, Reynhout S, Lenaerts L, Derua R, Houge G, Janssens V. Protein Phosphatase 2A (PP2A) mutations in brain function, development, and neurologic disease. Biochem Soc Trans 2021:BST20201313. [PMID: 34241636 DOI: 10.1042/BST20201313] [Cited by in F6Publishing: 2] [Reference Citation Analysis]